CN1617833A - Low water uptake silicas - Google Patents
Low water uptake silicas Download PDFInfo
- Publication number
- CN1617833A CN1617833A CNA028276280A CN02827628A CN1617833A CN 1617833 A CN1617833 A CN 1617833A CN A028276280 A CNA028276280 A CN A028276280A CN 02827628 A CN02827628 A CN 02827628A CN 1617833 A CN1617833 A CN 1617833A
- Authority
- CN
- China
- Prior art keywords
- medium
- silicate
- obtains
- souring agent
- silicon
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 46
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 295
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 141
- 238000000034 method Methods 0.000 claims abstract description 104
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 80
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims abstract description 52
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 42
- 238000001035 drying Methods 0.000 claims abstract description 16
- 239000012065 filter cake Substances 0.000 claims abstract description 16
- 239000012429 reaction media Substances 0.000 claims abstract description 15
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 10
- 239000010703 silicon Substances 0.000 claims abstract description 10
- 238000001914 filtration Methods 0.000 claims abstract description 7
- 239000002609 medium Substances 0.000 claims description 64
- 239000003795 chemical substances by application Substances 0.000 claims description 56
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 40
- 239000000203 mixture Substances 0.000 claims description 36
- 239000011159 matrix material Substances 0.000 claims description 31
- -1 aluminum compound Chemical class 0.000 claims description 23
- 239000007864 aqueous solution Substances 0.000 claims description 22
- 230000008569 process Effects 0.000 claims description 20
- 238000005507 spraying Methods 0.000 claims description 14
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 13
- 239000002994 raw material Substances 0.000 claims description 13
- 238000010521 absorption reaction Methods 0.000 claims description 11
- 239000012763 reinforcing filler Substances 0.000 claims description 10
- 239000000243 solution Substances 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 6
- 229910052910 alkali metal silicate Inorganic materials 0.000 claims description 6
- 239000000945 filler Substances 0.000 claims description 6
- 239000012736 aqueous medium Substances 0.000 claims description 4
- 238000005516 engineering process Methods 0.000 claims description 4
- 230000035800 maturation Effects 0.000 claims description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 4
- 239000008194 pharmaceutical composition Substances 0.000 claims description 4
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- 238000000465 moulding Methods 0.000 claims description 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 2
- 235000019253 formic acid Nutrition 0.000 claims description 2
- 229910017604 nitric acid Inorganic materials 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 230000008719 thickening Effects 0.000 claims description 2
- 230000036962 time dependent Effects 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract description 9
- 229920001971 elastomer Polymers 0.000 abstract description 2
- 239000002535 acidifier Substances 0.000 abstract 4
- 229910052681 coesite Inorganic materials 0.000 abstract 2
- 229910052906 cristobalite Inorganic materials 0.000 abstract 2
- 239000007858 starting material Substances 0.000 abstract 2
- 229910052682 stishovite Inorganic materials 0.000 abstract 2
- 229910052905 tridymite Inorganic materials 0.000 abstract 2
- 239000000806 elastomer Substances 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 230000003014 reinforcing effect Effects 0.000 abstract 1
- 229960001866 silicon dioxide Drugs 0.000 description 71
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 24
- 238000003756 stirring Methods 0.000 description 19
- 235000019353 potassium silicate Nutrition 0.000 description 15
- 239000002245 particle Substances 0.000 description 14
- 239000011734 sodium Substances 0.000 description 14
- 239000000843 powder Substances 0.000 description 11
- 239000004115 Sodium Silicate Substances 0.000 description 10
- 229910052911 sodium silicate Inorganic materials 0.000 description 10
- 239000001117 sulphuric acid Substances 0.000 description 10
- 235000011149 sulphuric acid Nutrition 0.000 description 10
- 229910052799 carbon Inorganic materials 0.000 description 9
- 150000003839 salts Chemical class 0.000 description 9
- 239000008188 pellet Substances 0.000 description 8
- 239000002002 slurry Substances 0.000 description 8
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- 238000002844 melting Methods 0.000 description 7
- 230000008018 melting Effects 0.000 description 7
- 238000001556 precipitation Methods 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- 238000005728 strengthening Methods 0.000 description 5
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 4
- 125000004429 atom Chemical group 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 150000001721 carbon Chemical group 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000000227 grinding Methods 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 239000011148 porous material Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 229910000077 silane Inorganic materials 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 3
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 125000001153 fluoro group Chemical group F* 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000006703 hydration reaction Methods 0.000 description 3
- 239000006072 paste Substances 0.000 description 3
- 239000002243 precursor Substances 0.000 description 3
- 229920002379 silicone rubber Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000005987 sulfurization reaction Methods 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 229910008051 Si-OH Inorganic materials 0.000 description 2
- 229910020175 SiOH Inorganic materials 0.000 description 2
- 229910006358 Si—OH Inorganic materials 0.000 description 2
- 238000005054 agglomeration Methods 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 238000007872 degassing Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 230000036571 hydration Effects 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 239000011810 insulating material Substances 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 125000000962 organic group Chemical group 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 238000005502 peroxidation Methods 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000012216 screening Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- NHOWDZOIZKMVAI-UHFFFAOYSA-N (2-chlorophenyl)(4-chlorophenyl)pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(Cl)C=C1 NHOWDZOIZKMVAI-UHFFFAOYSA-N 0.000 description 1
- QEQBMZQFDDDTPN-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy benzenecarboperoxoate Chemical compound CC(C)(C)OOOC(=O)C1=CC=CC=C1 QEQBMZQFDDDTPN-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical group C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- ZRNSSRODJSSVEJ-UHFFFAOYSA-N 2-methylpentacosane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCC(C)C ZRNSSRODJSSVEJ-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229910052684 Cerium Inorganic materials 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical group NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 239000004111 Potassium silicate Substances 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- DPDMMXDBJGCCQC-UHFFFAOYSA-N [Na].[Cl] Chemical compound [Na].[Cl] DPDMMXDBJGCCQC-UHFFFAOYSA-N 0.000 description 1
- NOZAQBYNLKNDRT-UHFFFAOYSA-N [diacetyloxy(ethenyl)silyl] acetate Chemical compound CC(=O)O[Si](OC(C)=O)(OC(C)=O)C=C NOZAQBYNLKNDRT-UHFFFAOYSA-N 0.000 description 1
- TVJPBVNWVPUZBM-UHFFFAOYSA-N [diacetyloxy(methyl)silyl] acetate Chemical compound CC(=O)O[Si](C)(OC(C)=O)OC(C)=O TVJPBVNWVPUZBM-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052936 alkali metal sulfate Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 1
- YLFIGGHWWPSIEG-UHFFFAOYSA-N aminoxyl Chemical compound [O]N YLFIGGHWWPSIEG-UHFFFAOYSA-N 0.000 description 1
- 229910052728 basic metal Inorganic materials 0.000 description 1
- 150000003818 basic metals Chemical class 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000031709 bromination Effects 0.000 description 1
- 238000005893 bromination reaction Methods 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 1
- RLGQACBPNDBWTB-UHFFFAOYSA-N cetyltrimethylammonium ion Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)C RLGQACBPNDBWTB-UHFFFAOYSA-N 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 description 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 125000003784 fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- 241000411851 herbal medicine Species 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 230000000887 hydrating effect Effects 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 238000006459 hydrosilylation reaction Methods 0.000 description 1
- 230000033444 hydroxylation Effects 0.000 description 1
- 238000005805 hydroxylation reaction Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N monofluoromethane Natural products FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- LHPDAPVJSKDGCA-UHFFFAOYSA-N n-ethyl-n-$l^{1}-oxidanylethanamine Chemical compound CCN([O])CC LHPDAPVJSKDGCA-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052757 nitrogen Chemical group 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 229920001558 organosilicon polymer Polymers 0.000 description 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 150000003057 platinum Chemical class 0.000 description 1
- 229910052913 potassium silicate Inorganic materials 0.000 description 1
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 150000003385 sodium Chemical class 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 239000000606 toothpaste Substances 0.000 description 1
- 229940034610 toothpaste Drugs 0.000 description 1
- 239000012745 toughening agent Substances 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000003828 vacuum filtration Methods 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
- 238000005550 wet granulation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B33/00—Silicon; Compounds thereof
- C01B33/113—Silicon oxides; Hydrates thereof
- C01B33/12—Silica; Hydrates thereof, e.g. lepidoic silicic acid
- C01B33/18—Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof
- C01B33/187—Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof by acidic treatment of silicates
- C01B33/193—Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof by acidic treatment of silicates of aqueous solutions of silicates
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
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Abstract
The invention concerns a method for preparing low water uptake precipitated silicas, comprising successive steps which consist in: (a) producing an initial starter including a silicate, the silicate concentration in said starter, expressed in SiO2 equivalent, being less than 15 g/L; (b) bringing the medium pH to a value ranging between 7 and 8 by adding an acidifying agent, (c) in the resulting medium, simultaneously adding a silicate and an acidifying agent the respective amounts of silicate and acidifying agent added in time being specifically such that, during the entire addition (1) the reaction medium pH stays between 7 and 8, and (ii) the silicon concentration in the medium, expressed in SiO2 equivalent, stays below 35 g/L; (d) adding an acidifying agent in the medium resulting from step (c), so as to bring the medium to a pH ranging between 3 and 6.5; and (e) filtering the resulting aqueous silica dispersion, then drying the filter cake obtained at the end of the filtering step. The invention also concerns low water uptake silicas obtained by said method and their use, in particular for reinforcing silicones or polymer or elastomer matrices.
Description
The present invention relates to prepare precipitated silica, especially powder, particle or substantially spherical pellet form, and have the method for the precipitated silica of low water absorption.The invention still further relates to gained precipitated silica and uses thereof, be particularly useful for strengthening the purposes of silicone elastomer or silicone paste matrix.
In silicone elastomer or silicone paste composition, pyrogenic silica, promptly, by comprising the silicon-dioxide that allows the tetrachloro silicane compounds at high temperature obtain with the method for hydrogen and oxygen reaction, as at for example Angewandte Chemie, the 72nd volume, those described in 744 pages (1960) used many years as reinforcing filler.
Yet because its acquisition methods, burning silicon-dioxide generally is expensive.For this reason, in the application that strengthens silicone matrix, paid effort soon, so that replace these expensive silicon-dioxide with so-called ' precipitation ' silicon-dioxide to small part, the former passes through by precursor, as silicate under suitable pH condition in aqueous medium precipitated silica obtain.These silicon-dioxide are cheap, and they can have required dispersing characteristic in silicone type matrix.
Yet, under most general case, usually find that precipitated silica has the intensive water affinity.This can find foundation from the fact of the mechanism used to small part described precipitation of silica process, this mechanism usually is complicated, poorly controlled phenomenon when generally having caused nucleation, grow and having solidified has caused having formed moisture absorption Si-OH group usually on the gained silica particles.
Generally, silicon-dioxide especially obtains reflection by its so-called ' water-intake rate ' feature to the avidity of water, and this has shown that more or less water molecules is adsorbed on its lip-deep significantly (marked) proneness.Generally, ' water-intake rate ' of silicon-dioxide is by comprising that the silica sample of dry (usually in low-down relative humidity and be higher than under 100 ℃ the temperature) is in advance placed the scheduled time under set relative humidity condition measure, the result, the silicon-dioxide hydration has caused that sample quality is increased to end value (m+dm) from initial value m (drying regime).' water-intake rate ' equals ratio dm/m corresponding to the water yield in the sample of being incorporated into based on the quality of drying regime sample, represents by percentage.
Therefore ' water-intake rate ' of silicon-dioxide be relative value, and this depends on drying and the hydrating condition that uses in the moisture content test of being carried out.In order to formulate the clearly definition of this feature in the present invention, in the remainder of whole narration, term ' water-intake rate of silicon-dioxide ' is used for specially representing that the dm/m that represents by percentage for the silica sample that stands following condition in process of the test is calculated compares:
-dry in advance: 8 hours, 105 ℃;
-hydration: 24 hours, 20 ℃, under 70% relative humidity.
Therefore, in order to measure ' water-intake rate ' of silicon-dioxide in the present invention, used experimental arrangement can typically comprise:
The silicon-dioxide that will test of the about 2g of-accurately weighing quality;
-with in the silica of the such weighing thermostat container under being set in 105 ℃ temperature dry 8 hours;
-measure the quality m of the dried silica that obtains by this drying step;
-the gained dried silica was placed 24 hours down at 20 ℃ in the encloses container (for example moisture eliminator) that contains the water/glycerol mixture with water/qualities of glycerin ratio of 35/65, make that the relative humidity of airtight medium is 70%;
-measure by the quality (m+dm) of silicon-dioxide of assigning this processings acquisition of 24 hours in 70% relative humidity, this quality is measured after silicon-dioxide leaves moisture eliminator immediately, so that avoid the quality of silicon-dioxide under the influence of the change of the humidity between medium under 70% the relative humidity and the laboratory air to occur changing.
According to definition of the present invention, prevailing precipitated silica generally has and is higher than 7%, the water-intake rate usually above 9%.Therefore, the water-intake rate of common precipitated silica generally is about 8-10%, seldom has precipitated silica to have and is lower than 6.5% water-intake rate.
When silicon-dioxide was used for strengthening silicone matrix, this avidity to water usually was tedious.Really, generally preferably, the silicon-dioxide that is used to strengthen silicone matrix is feature with the most weak as far as possible avidity to water.And under the particular case of the silicone elastomer that for example is used as the insulating material in the electric wire, necessary is that the silicon-dioxide that is used as filler contains the least possible water, especially in order not damage the dielectric properties of this material.
In addition, water is being easy to cause that as the existence in the silicon-dioxide of the reinforcing filler in the silicone matrix bubble forms in described matrix, when it when extruding moulding, this is unacceptable defective in extruding parts.
Known these factors so it is evident that, are wanted precipitated silica as the reinforcing filler in the silicone type matrix should not only have polymolecularity in described medium, and are had minimum possible water-intake rate value.
Yet the precipitated silica of prior art does not almost have these features.
To satisfy dispersed in silicone type matrix and, considered known high water absorbing capacity precipitated silica is handled, in order to provide so that reduce their avidities to water to the silicon-dioxide of the double requirements of the low-affinity of water.
In this respect, as described in the application FR 2 356 596, proposed for example to make the method for the surface hydrophobicity of precipitated silica, especially by using silane or silazane class agent.Yet handling, this class hydrophobization generally has high relatively cost.
Another terms of settlement of handling the high water absorbing capacity precipitated silica in being used for described in the application EP 0 280 623 is included in the inclination rotary oven at 700-950 ℃ of following heat treatment precipitation silicon-dioxide, preferably by using the initial silicon-dioxide of pellet form.Though this method cost is lower than the method for FR 2,356 596, yet still comprising, it implements two different steps, promptly prepare and subsequent disposal, this has increased cost in the industrial implementation field of this method.
Now, the inventor has been found that to have and is particularly useful for strengthening the dispersiveness of silicone type matrix and the precipitated silica of water-intake rate characteristic can be produced by the precipitation of silica method, do not need subsequent disposal gained precipitated silica.
More precisely, the inventor's work discloses, can produce and be presented at the intramatrical good dispersion of silicone type, and to be lower than 6% water-intake rate is the precipitated silica of feature, prerequisite is that the precipitin reaction of silicon-dioxide is carried out under controlled conditions, especially by in diluent media, carrying out precipitin reaction and by in the forming process of silicon-dioxide, the pH of reaction medium being remained on about 7.5 value.
For the water-intake rate value, the result who is obtained by the inventor is wonderful especially.In fact, the present best silicon-dioxide that obtains by the intermediate processing of prior art has the water-intake rate value of 6.5-7% at least.
Find that according to this one of purpose of the present invention provides the novel method of preparation precipitated silica, this method is used simple, economical, and can obtain to show the good distribution characteristic, especially in the intramatrical good dispersion of silicone type, and the silicon-dioxide of low-down avidity to water.
More specific is, another object of the present invention provides can be in silicone type polymeric matrix, especially at the precipitated silica that for example is used for being used as toughener in the coating of electric wire is guaranteed the silicone type elastomeric matrices of function of insulating material.
Therefore,, the present invention relates to prepare the method for low water absorption precipitated silica, comprise following consecutive steps according to first aspect:
(a) produce the initial feed that comprises silicate, the silicate concentration in described raw material is (with SiO
2Equivalent is represented) be lower than 15g/l;
(b), make the pH of medium reach the value of 7-8, the value of preferred 7.2-7.8, advantageously 7.3-7.7 (typically, equal substantially 7.5 value) by adding souring agent;
(c) in the gained medium, add silicate and souring agent simultaneously, specifically select the time dependent addition separately of silicate and souring agent, make in whole interpolation process:
The pH of-reaction medium remains on 7-8, advantageously 7.2-7.8; With
-silicon concentration in medium (is pressed SO
2Equivalent is represented) keep below or equal 35g/l;
(d) souring agent is joined in the medium that obtains by step (c), so that make medium be in the pH of 3-6.5; With
(e) filter gained aqueous silica dispersion and dry in the last filter cake that obtains of filtration step, preferably washing in advance;
Thereby obtained solid-state described low water absorption precipitated silica.
The silicate that uses in the step (a) of method of the present invention and (c) can be selected from the silicate of all common formats, especially metasilicate or bisilicate.It is desirable to, silicate used according to the invention is alkalimetal silicate, as water glass or potassium silicate.
In particularly preferred mode, the silicate of step (a) is water glass, and what add in step (c) also is water glass.In this case, used water glass is generally with 2-4, advantageously the SiO of 3-3.6
2/ Na
2The O weight ratio is a feature, this SiO
2/ Na
2The O weight ratio is 3.3-3.5 (general, this ratio equals 3.4 substantially) preferably.
The initial feed of the step of method of the present invention (a) exists with the form of aqueous silicate solution usually, is less than or equal to 15g/l its concentration feature.Typically, the silicate concentration in the raw material of step (a) is (with SiO
2Equivalent is represented) be 1g/l-15g/l.This silicate concentration in the raw material of step (a) is (with SiO
2Equivalent is represented) advantageously be less than or equal to 10g/l, preferably be less than or equal to 9g/l.
The raw material of step (a) generally has the pH of about 9-13.The step of method of the present invention (b) comprises particularly by adding souring agent and reduces this pH value, so that make the pH of this medium reach 7-8, the inventor is verified, and precipitation of silica is reflected at this scope to carry out in the best way.
Term on meaning of the present invention ' souring agent ' is meant any inorganic or organic acid compound of the pH that is easy to reduce raw material.Mineral acid, as sulfuric acid, hydrochloric acid or nitric acid, or organic acid, as acetate, therefore formic acid or carbonic acid can be advantageously used for souring agent.
Advantageously, in preparation in accordance with the present invention, especially in step (a), do not add ionogen.Term ' ionogen ' here uses with its common meaning, and promptly this term is meant any lewis' acid material, in the time of in being in solution, decomposing or splits, and forms ion or charged particle.Electrolytical example is the salt of basic metal and alkaline-earth metal, the salt of for example initial silicate metal and souring agent, and sodium-chlor (under the situation of water glass and hydrochloric acid reaction) for example, or preferentially be sodium sulfate (under the situation of water glass and vitriolic reaction).
The souring agent that uses in the step (b) of method of the present invention is sulfuric acid preferably, is alkalimetal silicate if especially be arranged in the silicate of initial feed.Generally, the souring agent of step (b) is introduced with the form of the aqueous solution usually, and preferred dilute aqueous soln generally has the equivalent concentration of 0.25N-8N.Therefore, in step (b), the pH of medium can advantageously have 10-350g/l by interpolation, and the aqueous sulfuric acid of the concentration of preferred 50-250g/l reduces.
Regardless of the exact nature of the souring agent of step (b), it must use so that its interpolation causes the mode that the pH of medium is reduced to the value of 7-8.The amount of the souring agent that uses is generally measured by the formation that is determined at pH in the interpolation process in practice, last till that from the interpolation of the souring agent of step (b) pH reaches desirable value till.
Advantageously, in the method for the invention, in step (b), reach 50-100 ℃ temperature in advance, preferably reach in the raw material of the temperature that is greater than or equal to 90 ℃ and reduce pH by souring agent is joined.
In addition, the interpolation of step (b) is preferably carried out gradually, promptly generally advantageously spends 3-60 minute, equals 5 minutes and preferably equaled at least 10 minutes interpolation time usually at least.Yet this interpolation time advantageously is less than 30 minutes.
A particular according to admissible step (b), this step can comprise maturing process, this randomly by allowing this medium with time of common 5-30 minute, preferably cultivates (develop) and carries out under 90-100 ℃ temperature, it should be understood that, after this slaking, conditioned reaction medium pH especially by adding souring agent, makes when step (b) finishes if desired, the pH of medium is positioned at the pH scope of 7-8, advantageously in above-mentioned preferable range.
In step (b) afterwards (by this step, make the pH of reaction medium reach the preferable range of 7-8, more preferably reach about 7.5), the step of method of the present invention (c) comprises proceeds precipitation of silica technology, by introducing other silicate, and specificly remain on 7-8, preferably under substantially invariable value by pH with medium, this steady state value promptly is generally 7.3-7.7 in this case preferably near 7.5.
For this reason, the silicate of step (c) is introduced with souring agent, adds the pH increase that silicate is found separately if the latter has offset.Preferably, the step of method of the present invention (c) is to obtain in the step (b) to carry out immediately after the required PH values.
Silicate that carries out in step (c) and souring agent ' adding simultaneously ' advantageously comprises and joins silicate in the medium continuously, measure the pH of medium and the value of regulating this pH by introducing souring agent simultaneously, for example, in case the pH of medium surpasses the trial value of 7-8, can introduce souring agent, this trial value generally is fixed on about 7.5.Like this, in this medium, keep substantially invariable pH value, i.e. near advantageously change fixed value+/-0.2pH unit (preferred+/-0.1pH unit), general 7.3-7.7.
Alternatively be, add in the time of step (c) and can also comprise and join souring agent in the medium continuously, pH regulates by introducing silicate in the interpolation process in this case, here also feasible is, for example, in case the pH of medium is reduced to 7-8, be fixed on usually below about 7.5 the controlling valu, introduce silicate.By this method, in medium, kept substantially invariable pH, i.e. near advantageously change fixed value+/-0.2pH unit (preferred+/-0.1pH unit), described value generally is 7.3-7.7.
According to another embodiment that it is contemplated that, interpolation can also comprise continuous interpolation souring agent and silicate in the time of step (c), and calculates its concentration and flow velocity, makes that the pH of medium remains on 7-8 in whole interpolation process, preferred 7.2-7.8.In this case, the pH of medium is general to be formed in step (c) process in often in remaining on above-mentioned scope, but in some cases, it can keep constant value, and advantageously about 7.5.Generally preferably, in step (c) instant flow velocity corresponding to the silicate official who is introduced can (NaOH with molar equivalent represents) (mark d in amount/second
S) and the sour functional amount (mol) introduced/second (mark d
A), and should make d
S/ d
ARemain on 1.01-1.09 than forever, preferred 1.02-1.07.
Regardless of carrying out step (c) blanking method really, used silicate and souring agent are identical with used those in step (a) and (b) usually.From therefore alkalimetal silicate preferably of the silicate of step (c), water glass advantageously, and souring agent preferably inorganic acid, sulfuric acid usually.
Because the silicon concentration in medium is (with SiO
2Equivalent is represented) must in step (c), keep below to characteristic in the interpolation process or equal 35g/l, so be incorporated into silicate in the reaction medium generally with dilute aqueous soln in step (c), promptly concentration is (with SiO
2Equivalent is represented) advantageously be preferably to be lower than 300g/l by 10-360g/l, the form that advantageously is lower than the solution of 270g/l exists; When using alkalimetal silicate such as water glass, situation is especially true.Similarly, souring agent exists with the form of dilute aqueous soln usually, and it generally has 0.25-8N, the equivalent concentration of preferred 0.5-4N.Therefore, the souring agent of employed therein step (c) is under the particular case of aqueous sulfuric acid, and the concentration of this solution advantageously is 25-380g/l, preferred 50-300g/l.
Should be emphasized that, if use dilute concentration at the medium that is used for by the method according to this invention precipitated silica, so especially, the salt concn characteristic earth polar of getting in touch with the reacting phase of silicate and souring agent in this medium is low, and this has caused the low ionic strength in used precipitation medium.
Do not wish to be subjected to by any way the constraint of particular theory, plausiblely be, by checking pH used according to the invention and concentration, the formation of SiOH surface group can be minimized, and in the method for the prior art of not taking this inspection, generally formed this a large amount of SiOH surface groups.Therefore the present invention can obtain to have the precipitated silica of utmost point low water absorption.
For in addition more effectively monitor the formation of silicon-dioxide, the inventor confirms, particularly advantageously is, add when carrying out step (c) with low relatively silicate and souring agent flow velocity, that is, usually, the interpolation time of step (c) is preferably 15-300 minute, more preferably 30-100 minute.This interpolation time has generally obtained to have the silica dioxide granule of extremely low Si-OH surface group content.
Generally, the step of method of the present invention (c) is advantageously carried out when stirring, preferably under 50-100 ℃ temperature, and usually under the temperature identical with the interpolation of step (b).The temperature of carrying out step (c) therefore can advantageously be 90-100 ℃, preferably about 95 ℃.
A particular variant of the method according to this invention, in the process of step (c), preferably (promptly at the end of this step, typically, corresponding to this step last 1/4th during, generally last 5-15 minute of this step) can be with al-based compound, the salt of preferred acidic, as Tai-Ace S 150, perhaps basic cpd is incorporated in the reaction medium as sodium aluminate.The interpolation of this al-based compound especially can cause the improvement of gained silicon-dioxide water-intake rate characteristic, and is using under the particular case of sulfuric acid as souring agent, and this can reduce the sulphate content in the silicon-dioxide that obtains when method of the present invention finishes.The introducing amount of aluminum compound generally makes the Al/SiO in reaction medium
2Ratio is 0.1-1 quality %, and this ratio preferably equals 0.6% at the most, preferably is less than or equal to 0.5%.
Really execute scheme conscientiously regardless of step (c), specific at the pH of the reaction medium at this step end is 7-8, preferably approximately 7.5.
Become with the desired application of silicon-dioxide with method preparation of the present invention, the step (d) that its medium is acidified to the pH scope of 3-6.5 can change according to the addition of souring agent.Preferably, this medium had reached the pH of 3.5-5.5 before step (d) finishes.
The souring agent of step (d) whether with in step (b) and those souring agents that use (c) identical or different be unessential.Preferably, this souring agent of step (d) form with the centinormal 1 aqueous solution with 0.25-8N is incorporated in the medium.Advantageously, it is an aqueous sulfuric acid, depends on the circumstances generally to have the concentration of 25-380g/l.
Carry out normally 50-100 ℃ of the temperature of optional step (d), it therefore can be identical with the temperature of using in previous step (c).
Usually, in entire method, if the step (a) and (b) of this method, (c) and (d) all under 90-100 ℃ temperature, advantageously under 93-97 ℃ temperature, also more advantageously carrying out under 95 ℃ the temperature equaling substantially, so also is preferred.
An advantageous embodiment of the method according to this invention, can carry out maturation stage by step (c) and the aqueous silica dispersion that (d) obtains, suitable words, usually by allowing this medium under 90-100 ℃ temperature, keep advantageously for 15-240 minute, preferably the time that surpasses 30 minutes carries out, preferably stir simultaneously, temperature in maturing process is preferably substantially invariable (if suitably, advantageously equal 95 ℃ substantially), or in 90-100 ℃ temperature range, raise (in one or more stages, depending on the needs usually).
Should be emphasized that, can be at the aluminum compound of the last interpolation of step (c), especially the Tai-Ace S 150 compounds can also add in step (d), perhaps adds in follow-up maturation stage (when carrying out this step).Therefore al-based compound can join in the medium between step (c) and the step (e) usually.
The step of method of the present invention (e) comprises the silicon-dioxide that reclaims solid form from the dispersion that previous step obtains generally.
In this step (e), usually filter with pressure filter by the dispersion that obtains in step (d) and the optional follow-up maturation stage, or use rotary filter, belt filter or flat filter to carry out vacuum filtration, this filtration has obtained " silica filter cake ", promptly has the silica slurry of relative high water content.The gained silica filter cake is carried out washing step then usually, generally makes water, so that reduce its salts contg, carry out drying then, especially use the spraying that is fit to form, for example use the turbine spray dispenser, the nozzle spray divider, hydraulic atomizing divider, or two-fluid spray dispenser.
Silica filter cake generally divides in advance, has the feasible abundant low viscous silica slurry that can be pumped into spray dispenser so that form.This slurry has preferably shown the melting loss of being less than or equal to 82 quality % under 1,000 ℃.
Splitting method for example can be chosen wantonly by in the shredder of filter cake being put into colloidal mill or ball mill class, or by using ultrasonic fragmentation to carry out.Especially, if filter cake obtains by filtering with pressure filter, advantageously in step toward division, use the stirring means with high shear force, the stirring means of for example reverse type.It is contemplated that the interpolation al-based compound, so that help dividing operation.
The low viscosity slurry that is obtained by this division is generally the aqueous silica dispersion form, and it directly is pumped in the spray dispenser of step (e).Yet, carry out after step (e) it is also conceivable that, especially in different working spaces (active site).The low viscosity slurry that obtains after division in most of the cases is the water-based silicon dioxide compositions, it is convenient to transportation and stores, and can be at any time under the effect of mechanical stress fully, become have the fluid viscosity that enough is used for pumping the silica dispersion form, dry by spraying then.The invention particularly relates to this specific water-based silicon dioxide compositions.
The precipitated silica that obtains with method of the present invention can be preferably 80-350 μ m with mean diameter, and advantageously the substantially spherical pellet form of 150-280 μ m exists, if especially it has the division filter cake that is lower than 82% melting loss by drying and obtains.The mean particle size of this pellet is measured by drying screening with by measuring corresponding to the diameter of 50% built up residue according to standard NF X 11507 (in December, 1970).The tamped density of the occupied state (DRT) of this class pellet of measuring according to standard NF T 30 042 generally is at least 0.2, typically 0.25-0.3.And these pellets have 3cm at least usually
3/ g, advantageously 3.5-4.5cm
3The total pore volume of/g, this pore volume uses mercury porosimeter to measure (specimen under 200 ℃ in thermostat container dry 2 hours, under vacuum, outgas immediately in after it leaves thermostat container 5 minutes then), and bore dia use WASHBURN ratio, calculate (MICROMERITICS 9300 porosity meters) with the contact angle θ that equals 140 ° with the surface tension γ that equals 484 dyne/cm.
This class pellet can carry out follow-up grinding, so that obtain the precipitated silica of powder form, wherein particle can have the mean particle size of 3-15 micron, depends on the intensity of grinding.
More generally, depend on the exsiccant type of being carried out, the precipitated silica that is obtained by step (e) can be isotropy or anisotropic particle powder form, has the average dimension that is generally the 3-350 micron.The tamped density of the occupied state (DRT) of these powders of measuring according to standard NF T 30 042 generally is 0.1-0.3.And it advantageously is 3-6cm that these powders have usually
3/ g as above total pore volume for pellet definition.
In the specific preparation that is used for strengthening the silicon-dioxide of silicone type matrix, the silicon-dioxide that produce preferably is the 3-30 micron with the mean particle size, and the particle form of preferred 5-15 micron exists.In order to obtain this granularity, can use the silicon-dioxide of any kind that obtains by method of the present invention, and the grinding steps of choosing wantonly; The different grain size of finding in gained silicon-dioxide if necessary can use the vibrating strainer that for example has suitable mesh size to separate then, can reclaim too big particle and they are turned back in the grinding.
Can also carry out agglomeration step by the dried silica that step (e) obtains, especially by directly compression, by wet granulation (promptly using binding agent), by extruding with preferably real by dry-pressing as water.If use this last a kind of technology, verified, advantageously, before the beginning compacting with powdered product degasification (technology that also is called pre-closeization or the degassing), so that eliminate the air wherein contain and more uniform compacting is provided.Last in agglomeration step can be classified as desired particle size with product, for example by screening, prepares to be used for subsequent applications then.The precipitated silica of the compacting that can obtain according to this particular according to the present invention advantageously exists with particle form.These particles are optional can to have the shape of maximum difference.Example comprises sphere (polylobe), and is cylindrical, parallelepiped, rhombus, sheet and ball-shape, and the shape of extruding with circle or multiple leaf-shaped section.These particulate mean sizess are 2-20mm preferably.And the tamped density of the described particles filled state of measuring according to standard NF T 30042 generally is at least 0.15, and can be up to 0.35, and these particles generally have 2.5-4.5cm
3The total pore volume of/g.
Regardless of shape, the precipitated silica that is obtained by method of the present invention generally has the low-down water-intake rate on meaning of the present invention, especially with big specific surface area and low density, this has given them with polymolecularity, especially in silicone type elastomeric matrices, and this makes them especially be suitable as reinforcing filler in the silicone type matrix.
Therefore, method of the present invention has obtained to have the precipitated silica that is lower than 6% water-intake rate usually.Should remember that the water-intake rate of mentioning is the water-intake rate on the meaning of the present invention measured of the drying/hydration test according to above regulation here.In most of the cases, the water-intake rate of the silicon-dioxide that obtains with method of the present invention is less than or equal to 5.9%, is usually less than 5.8%.Therefore the water-intake rate of the silicon-dioxide that obtains with method of the present invention especially can advantageously be less than or equal to 5.7%, even is less than or equal to 5.5%.Advantageously, it is less than or equal to 5.4%, and even is less than or equal to 5.3%.Yet under most of general cases, it more specifically is higher than 4.5% usually above 4%.
Except this low water absorption, the silicon-dioxide that obtains with method of the present invention generally should make, after 105 ℃ of following thermal treatments 8 hours, they have generally the 2-4 quality % based on the total mass of sample, preferably be lower than 3 quality %, advantageously be lower than 2.7% content of residual water based on the sample total mass based on the total mass of sample.
And the precipitated silica that obtains with method of the present invention generally has the 100m of being higher than
2/ g preferably equals 120m at least
2The BET specific surface area of/g is used at the Journal of theAmerican Chemical Society, vol.60, and the BRUNAUER-EMMET-TELLER method described in 309 pages (in December, 1938) is measured.This BET specific surface area advantageously equals 150m at least
2/ g, but it keeps below usually or equals 200m
2/ g.Therefore it generally be 120-185m
2/ g.
The silicon-dioxide that obtains with method of the present invention can also characterize with so-called CTAB specific surface area, and it is measured by the absorption according to the bromination hexadecyl trimethyl ammonium (pH=9) of standard NFT 45007 (in November, 1987).Generally, the CTAB specific surface area of the silicon-dioxide that obtains with method of the present invention is 100-200m
2/ g, it advantageously equals 110m at least
2/ g preferably equals 130m at least
2/ g.It is 120-185m typically therefore
2/ g.
In addition, the silicon-dioxide that obtains with method of the present invention is generally with 150ml/100g-300ml/100g, and the DOP oil number that preferably is higher than 200ml/100g is a feature, uses dioctyl phthalate (DOP) to measure according to standard NF T 30-022 (March nineteen fifty-three).
The precipitated silica that is obtained by method of the present invention generally contains the salt that acidulant employed forms the effect of used silicate that passes through of trace at least.Therefore, if method of the present invention is specifically used the precursor of alkalimetal silicate as silicon-dioxide, and use sulfuric acid as souring agent, precipitated silica contains alkali metal sulfates so.Generally, alkali metal sulphuric acid salts contg in gained silicon-dioxide is low relatively, usually make existing sulfate ion fair be 0.5 quality % at the most, based on the total mass of dry-matter (typically 0.1-0.5 quality %, based on the total mass of dry-matter).This sulfate ion content can also reduce by filtering after silica filter cake pressurization washing in the process of the step (e) of this method.In this case, the fair of existing sulfate ion is 0.05-4 quality %, based on the total mass of dry-matter, and advantageously be lower than 0.3 quality %, preferably be lower than 0.2 quality %, also more advantageously be lower than 0.1 quality %, based on the total mass of dry-matter.
If use the precursor of water glass in the method for the invention as silicon-dioxide, no matter use the souring agent of what type, the silicon-dioxide that is obtained by this method specifically contains sodium ion.Generally, the residual sodium content in gained silicon-dioxide is 300-1,500ppm, and this content can be less than or equal to 1, and 000ppm advantageously is less than or equal to 800ppm.This sodium content is launched by the flame spectrum that is dissolved in the silica sample with quality measurement in the hydrofluoric acid and is measured.
And silicon-dioxide of the present invention is with general 4.5-7, and the pH of preferred 4.8-6 is a feature, measures (pH of the 5 quality % suspension of silicon-dioxide in water) according to standard ISO 787/9.
The precipitated silica that obtains with method of the present invention has shown very good dispersive ability, they are particularly suitable for as the reinforcing filler in the silicone type matrix, they have given this matrix with very good rheologic behavio(u)r, provide very gratifying mechanical property for this matrix simultaneously.The present invention especially also relates to the purposes of the silicon-dioxide that is obtained by method of the present invention.
Therefore can particularly advantageously be applied to strengthen silicone type elastomeric matrices with prepared according to the methods of the invention silicon-dioxide, for example can cold vulcanization or heat-vulcanized elastomeric matrices.
Especially be suitable as the filler of silicon composition with the silicon-dioxide of method acquisition of the present invention.
Can not important with the type of the silicon-dioxide enhanced silicon composition that obtains by method of the present invention.Generally, these silicon compositions can be elastomeric-type or cream type.
Under the situation of elastic composition, generally use the vulcanizable silicone polymkeric substance, make that the sum of radicals R and the ratio of Siliciumatom sum are 0.5-3, wherein R represents to be bonded in the hydro carbons group of Siliciumatom.In the composition of organosilicon polymer, the available valency bond of other of silicon is connected to heteroatoms such as oxygen or nitrogen, or the multivalence alkyl.
Preferably, with the silica-filled silicon composition that obtains by method of the present invention is organopolysiloxane composition, wherein organopolysiloxane can be linearity or branching, and optional alkyl or the active group of also comprising, hydroxyl for example, hydrolysable group, alkenyl or hydrogen atom.
More precisely, the principal constituent organopolysiloxane of these compositions comprises the siloxane unit with following general formula:
With optional siloxane unit with following general formula:
In these general formulas, various symbols have following implication:
-R represents non-water-disintegrable hydro carbons group, and wherein this group can be:
-have 1-5 carbon atom and contain the alkyl or the haloalkyl of 1-6 chlorine and/or fluorine atom;
-have 3-8 carbon atom and contain the cycloalkyl or the halogenated cycloalkyl of 1-4 chlorine and/or fluorine atom;
-have 6-8 carbon atom and contain the aryl and the halogenated aryl of 1-4 chlorine and/or fluorine atom;
-have a cyano group alkyl of 3-4 carbon atom;
-Z represents hydrogen atom, alkenyl, hydroxyl, hydrolyzable atom, and hydrolysable group;
-n represents to equal 0,1,2 or 3 integer;
-x represents to equal 0,1,2 or 3 integer;
-y represents to be less than or equal to 2 integer.
The example that directly is bonded in the organic group R of Siliciumatom comprises following group: methyl; Ethyl; Propyl group; Sec.-propyl; Butyl; Isobutyl-; α-amyl group; The tertiary butyl; Chloromethyl; Dichloromethyl; α-chloroethyl; α, β-Dichloroethyl, methyl fluoride; Difluoromethyl; α, β-two fluoro ethyl; Three fluoro-3,3, the 3-propyl group; The trifluoro cyclopropyl; Cyclopropyl; Three fluoro-4,4, the 4-butyl; Seven fluoro-3,3,4,4,5, the 5-amyl group; The beta-cyano ethyl; γ-cyano group propyl group; Phenyl; Rubigan; Between chloro-phenyl-; Two chloro-3, the 5-phenyl; Trichlorophenyl; The tetrachloro phenyl; Adjacent, to or a tolyl; α, α, α-fluoroform phenyl; Dimethylbenzene such as dimethyl-2, the 3-phenyl; Dimethyl-3, the 4-phenyl.
Preferably, the organic group that is bonded in Siliciumatom is a methyl, phenyl or vinyl, and wherein these groups can be chosen wantonly by halogenation, or the cyano group alkyl.
The Z symbol is advantageously represented hydrogen or chlorine atom, vinyl, and hydroxyl or hydrolysable group, as amino, amide group, amino oxygen base, oxime, alkoxyl group, alkoxyl group alkoxyl group, alkenyl oxy acyloxy.
The type of organopolysiloxane is with therefore siloxane unit (I) and ratio (II) and described unitary distribution are generally used according to purpose and selected according to the sulfidizing that composition is carried out.
Therefore they can be at organo-peroxide, as peroxidation two chloro-2, the 4-benzoyl, benzoyl peroxide, t-butylperoxyl benzoate, under the effect of peroxidation cumyl and ditertiary butyl peroxide under heating up vulcanizable component.
Therefore the organopolysiloxane that is included in this based composition consists essentially of siloxane unit (I), does not contain any hydrolyzable group or atom.
Represented the example of industrial such particularly important with the poly-methyl polysiloxane of trimethyl silyl terminal.
Sulfuration can also undertaken by the cross-link bond that is created between vinyl silyl and the hydrogenation silyl under envrionment temperature or the neutral temperature, and this hydrosilylation reactions carries out in the presence of catalyzer such as platinum derivatives.Used organopolysiloxane does not contain hydrolyzable atom or group so.
Sulfuration can be carried out under the effect of moisture.The organopolysiloxane that contains in this based composition contains hydrolyzable atom or group, as those of above definition.The siloxane unit (II) that contains this class group accounts for the 15wt% at the most of used organopolysiloxane total mass.This class organopolysiloxane composition generally contains catalyzer, as pink salt.
Sulfuration can be carried out in the presence of linking agent at last.The organopolysiloxane that is included in these compositions generally is to comprise unit (I) and linearity (II), branching or cross linking polysiloxane, and wherein Z is that hydroxyl and x equal 1 at least.This linking agent can be multifunctional silane, as methyl triacetoxysilane, and sec.-propyl triacetoxysilane, vinyltriacetoxy silane, or methyl three (diethylamino oxygen base) silane.Various other compounds can be used as linking agent as silicate.
Silicon composition according to the present invention contains 5-50%, the precipitated silica as the optionally treating of above definition of preferred 10-40%.Under the situation of silicone paste, the ratio of silicon-dioxide of the present invention generally is 3-20%.
Except polysiloxane, the precipitated silica of optionally treating, beyond linking agent and the crosslinking catalyst, in addition, said composition can contain common fillers, as silica powder, diatomite, talcum, carbon black, or carbonate.Said composition can also contain various ordinary adjuvants, as anti-structurising agent, thermo-stabilizer, thixotropic agent, pigment and corrosion inhibitor.
Anti-structurising agent also is called as softening agent, generally is organosilicon character, and introduces with the ratio of the organic silica gel of 0-20 part/100 part.They have prevented that said composition from hardening in storage process.The example of anti-structurising agent comprises the silane with hydrolysable group, or has low-molecular-weight hydroxylation or alkoxylate diorganopolysiloxaneand.This based composition for example is described in French Patent FR-A-1, in 111,969.
The example that well known to a person skilled in the art thermo-stabilizer comprises salt, oxide compound and the oxyhydroxide of iron, cerium or manganese.These additives that can be used alone or as a mixture are generally introduced with the ratio based on the 0.01-5% of the weight of used organopolysiloxane glue.
Organopolysiloxane composition prepares by the various components of aforesaid said composition are mixed.Mixing can be carried out at ambient temperature, or carries out under heating.
Before crosslinked, silicone type matrix can be by extruding moulding.The silicon-dioxide that obtains according to the present invention is verified, can be effective as especially by the reinforcing filler in this silicone type matrix of extrusion moulding, and their low water content has limited the formation of bubble.
Except its application as the filler in the silicone type matrix, low water absorption silicon-dioxide of the present invention can also be advantageously used for the reinforcing filler in the organic polymer type matrix, particularly based on the matrix of one or more elastomericss (can be natural or synthetic), especially rubber-type matrix, more specifically based on the matrix of natural or synthetic rubber, the also more specifically reinforcing filler in SBR or the butyl type rubber matrix.The silicon-dioxide that obtains by method of the present invention shown the good dispersion in polymkeric substance and elastomeric matrices and strengthened characteristic, and wherein they especially can increase wear resistance, and this can prove favourable in pneumatic composition.
On elastomeric matrices enhanced meaning, the inventor is verified, the silicon-dioxide that obtains with method of the present invention is particularly suitable for strengthening transparent or semitransparent matrix, as be particularly useful for preparing those matrix of transparent or semitransparent rubber boots parts (for example heel), wherein they are more much smaller than other at present known silicon-dioxide that use in this respect of great majority for the influence of the transparency or translucency characteristic.
Low water absorption silicon-dioxide of the present invention can also be advantageously used in organic or the aqueous medium, preferred aqueous medium, the especially thickening material in the toothpaste.
In addition, the silicon-dioxide that obtains according to the present invention also proves useful in many other common application fields of precipitated silica, for example be used to produce paint vehicle or paper.Their verified carriers that can particularly advantageously be used as in food or the make-up composition.
Because their salts contg is low, so the silicon-dioxide that obtains with method of the present invention also is particularly suitable for the herbal medicine pharmaceutical field.Therefore silicon-dioxide of the present invention be particularly suitable as filler, carrier and/or the excipient in the pharmaceutical composition.The present invention especially also relates to silicon-dioxide of the present invention in the application aspect this, and thus obtained pharmaceutical composition.
A plurality of embodiment by following elaboration can know theme of the present invention and advantage more.
Embodiment 1
With 14, (236g/l presses SiO to the sodium silicate aqueous solution of 000g water and 630g
2The equivalent meter) is incorporated into the system that controlled temperature and pH are housed and have in the reactor of stirring system of three bladed propeller the SiO of used water glass
2/ Na
2O weight ratio (wr) is 3.46.
Beginning to stir (250rpm) afterwards, the raw material that forms like this is heated to 95 ℃, and at 11 minutes pH is transferred to 7.5 by the vitriolic aqueous solution (mean flow rate of 61g/min) that adds 80g/l.
In case reach 7.5 pH, add 4 continuously with the constant flow rate of 48g/min, 320g presses SiO
2The sodium silicate aqueous solution (wr=3.46) of equivalent meter 236g/l (adding the time length: 90 minutes), join in this medium pH with this medium by the aqueous sulfuric acid with 80g/l and remain on and equal 7.5 value (not exceeding 0.1pH unit), wherein flow velocity is monitored according to the variation of the pH of measured medium.Altogether, with 4, the 770g sulphuric acid soln joins in the medium, this sulphuric acid soln that is added corresponding to 53g/minute mean flow rate.
After 90 minutes interpolation, no longer add silicate, and add acid, be stabilized in 3.4 up to the pH of reaction medium.Allow the slaking 5 minutes when stirring of this solution then.
The gained slurry filters with flat filter then, and the gained filter cake is equaling mechanical disintegration under 5 the pH, and is dry by spraying then.
Gained exsiccant silicon-dioxide has shown following physics-chem characteristic:
The pH:5.5 of powder
Na
2SO
4Content: 0.2 quality % (based on the total mass of dry state material)
CTAB specific surface area: 160m
2/ g
BET specific surface area: 160m
2/ g
Melting loss under 1,000 ℃: 4.9%
Handle 2 hours content of residual water afterwards down at 1,000 ℃: 2.6%
Water-intake rate (according to definition of the present invention): 5.5%
Embodiment 2
With 14, (236g/l presses SiO to the sodium silicate aqueous solution of 000g water and 450g
2The equivalent meter) is incorporated into the system that controlled temperature and pH are housed and have in the reactor of stirring system of three bladed propeller the SiO of used water glass
2/ Na
2O weight ratio (wr) is 3.46.
Beginning to stir (250rpm) afterwards, the raw material that forms like this is heated to 98 ℃, and in 11 minutes, pH is transferred to 7.5 by the vitriolic aqueous solution (mean flow rate of 61g/min) that adds 80g/l.
In case reach 7.5 pH, add 3 continuously with the constant flow rate of 35g/min, 150g presses SiO
2The sodium silicate aqueous solution (wr=3.46) of equivalent meter 236g/l (adding the time length: 90 minutes), join in this medium pH with this medium by the aqueous sulfuric acid with 80g/l and remain on and equal 7.5 value (not exceeding 0.1pH unit), wherein flow velocity is monitored according to the variation of the pH of measured medium.Altogether, with 3, the 510g sulphuric acid soln joins in the medium, this corresponding to sulphuric acid soln that 39g added/minute mean flow rate.
After 90 minutes interpolation, no longer add silicate, and add acid, be stabilized in 3.4 up to the pH of reaction medium.Allow the slaking 5 minutes when stirring of this solution then.
The gained slurry filters with flat filter then, and the gained filter cake is equaling mechanical disintegration under 5 the pH, and is dry by spraying then.
Gained exsiccant silicon-dioxide has shown following physics-chem characteristic:
The pH:5.2 of powder
Na
2SO
4Content: 0.3 quality % (based on the total mass of dry state material)
CTAB specific surface area: 164m
2/ g
BET specific surface area: 165m
2/ g
Melting loss under 1,000 ℃: 4.8%
Handle 2 hours content of residual water afterwards down at 1,000 ℃: 2.6%
Water-intake rate (according to definition of the present invention): 5.5%
Embodiment 3
With 11, (236g/l presses SiO to the sodium silicate aqueous solution of 000g water and 630g
2The equivalent meter) is incorporated into the system that controlled temperature and pH are housed and have in the reactor of stirring system of three bladed propeller the SiO of used water glass
2/ Na
2O weight ratio (wr) is 3.46.
Beginning to stir (250rpm) afterwards, the raw material that forms like this is heated to 95 ℃, and at 11 minutes pH is transferred to 7.5 by the vitriolic aqueous solution (mean flow rate of 61g/min) that adds 80g/l.
In case reach 7.5 pH, add 4 continuously with the constant flow rate of 48g/min, 320g presses SiO
2The sodium silicate aqueous solution (wr=3.46) of equivalent meter 236g/l (adding the time length: 90 minutes), join in this medium pH with this medium by the aqueous sulfuric acid with 80g/l and remain on and equal 7.5 value (not exceeding 0.1pH unit), wherein flow velocity is monitored according to the variation of the pH of measured medium.Altogether, with 4, the 770g sulphuric acid soln joins in the medium, this sulphuric acid soln that is added corresponding to 53g/minute mean flow rate.
After 90 minutes interpolation, no longer add silicate, and add acid, be stabilized in 3.4 up to the pH of reaction medium.Allow the slaking 5 minutes when stirring of this solution then.
The gained slurry filters with flat filter then, and the gained filter cake is equaling mechanical disintegration under 5 the pH, and is dry by spraying then.
The gained dried silica has shown following physics-chem characteristic:
The pH:5.4 of powder
Na
2SO
4Content: 0.2 quality % (based on the total mass of dry state material)
CTAB specific surface area: 110m
2/ g
BET specific surface area: 126m
2/ g
Melting loss under 1,000 ℃: 5.1%
Handle 2 hours content of residual water afterwards down at 1,000 ℃: 2.7%
Water-intake rate (according to definition of the present invention): 5.2%
Embodiment 4
With 14, (236g/l presses SiO to the sodium silicate aqueous solution of 000g water and 450g
2The equivalent meter) is incorporated into the system that controlled temperature and pH are housed and have in the reactor of stirring system of three bladed propeller the SiO of used water glass
2/ Na
2O weight ratio (wr) is 3.46.
Beginning to stir (250rpm) afterwards, the raw material that forms like this is heated to 95 ℃, and at 11 minutes pH is transferred to 7.5 by the vitriolic aqueous solution (mean flow rate of 61g/min) that adds 80g/l.
In case reach 7.5 pH, add 3 continuously with the constant flow rate of 35g/min, 150g presses SiO
2The sodium silicate aqueous solution (wr=3.46) of equivalent meter 236g/l (adding the time length: 90 minutes), join in this medium pH with this medium by the aqueous sulfuric acid with 80g/l and remain on and equal 7.5 value (not exceeding 0.1pH unit), wherein flow velocity is monitored according to the variation of the pH of measured medium.Altogether, with 3, the 500g sulphuric acid soln joins in the medium, this corresponding to sulphuric acid soln that 40g added/minute mean flow rate.
After 90 minutes interpolation, no longer add silicate, and add acid, be stabilized in 3.4 up to the pH of reaction medium.Allow the slaking 5 minutes when stirring of this solution then.
The gained slurry filters with flat filter then, and the gained filter cake is equaling mechanical disintegration under 5 the pH, and is dry by spraying then.
Gained exsiccant silicon-dioxide has shown following physics-chem characteristic:
The pH:5.4 of powder
Na
2SO
4Content: 0.2 quality % (based on the total mass of dry state material)
CTAB specific surface area: 121m
2/ g
BET specific surface area: 131m
2/ g
Melting loss under 1,000 ℃: 5.4%
Handle 2 hours content of residual water afterwards down at 1,000 ℃: 2.7%
Water-intake rate (according to definition of the present invention): 5.2%
Embodiment 5
(236g/l presses SiO with 950L water and 33L sodium silicate aqueous solution
2The equivalent meter) is incorporated into the system that controlled temperature and pH are housed and have in the reactor of stirring system of three bladed propeller the SiO of used water glass
2/ Na
2O weight ratio (wr) is 3.46.
Beginning to stir (250rpm) afterwards, the raw material that forms like this is heated to 95 ℃, and in 11 minutes, pH is transferred to 7.5 by the vitriolic aqueous solution (mean flow rate of 219L/h) that adds 80g/l.
In case reach 7.5 pH, with the constant flow rate of 205L/h add continuously 290L by SiO
2The sodium silicate aqueous solution (wr=3.46) of equivalent meter 236g/l (adding the time length: 85 minutes), join in this medium pH with this medium by the aqueous sulfuric acid with 80g/l and remain on and equal 7.5 value (not exceeding 0.2pH unit), wherein flow velocity is monitored according to the variation of the pH of measured medium.Altogether, the 375L sulphuric acid soln is joined in the medium, this sulphuric acid soln that is added corresponding to 265L/minute mean flow rate.
After 85 minutes interpolation, no longer add silicate, and add acid, be stabilized in 3.4 up to the pH of reaction medium.Allow the slaking 5 minutes when stirring of this solution then.
The gained slurry filters with flat filter then, and the gained filter cake is equaling mechanical disintegration under 5 the pH, and is dry by spraying then.
Gained exsiccant silicon-dioxide has shown following physics-chem characteristic:
The pH:5.1 of powder
Na
2SO
4Content: 0.28 quality % (based on the total mass of dry state material)
CTAB specific surface area: 157m
2/ g
BET specific surface area: 165m
2/ g
Melting loss under 1,000 ℃: 5.4%
Handle 2 hours content of residual water afterwards down at 1,000 ℃: 3.1%
Water-intake rate (according to definition of the present invention): 5.7%
Claims (27)
1, the method for preparing the low water absorption precipitated silica comprises following consecutive steps:
(a) produce the initial feed that comprises silicate, the silicate concentration in described raw material is with SiO
2Equivalent represents to be lower than 15g/l;
(b), make the pH of medium reach the value of 7-8 by adding souring agent;
(c) in the gained medium, add silicate and souring agent simultaneously, specifically select the time dependent addition separately of silicate and souring agent, make in whole interpolation process:
The pH of-reaction medium remains on 7-8;
-silicon concentration in medium represents to keep below or equal 35g/l by the SO2 equivalent;
(d) souring agent is joined in the medium that obtains by step (c), so that make medium be in the pH of 3-6.5; With
(e) filter the gained aqueous silica dispersion, dry then at the last filter cake that obtains of filtration step.
2,, be characterised in that in step (a) and the silicate that uses (c) is alkalimetal silicate according to the method for claim 1.
3,, be characterised in that in step (b), (c) and the souring agent that uses (d) is selected from sulfuric acid, hydrochloric acid, nitric acid, acetate, formic acid and carbonic acid according to the method for claim 1 or claim 2.
4, according to each the method for claim 1-3, the raw material that is characterised in that step (a) is to have by SiO
2The form of the aqueous silicate solution of the concentration of being less than or equal to 10g/l that equivalent is represented exists.
5, according to each the method for claim 1-4, the souring agent that is characterised in that step (b) is introduced with the form of the centinormal 1 aqueous solution with 0.25-8N.
6, according to each the method for claim 1-5, the souring agent that is characterised in that step (b) is the sulfuric acid of introducing with the form of the aqueous solution of the concentration with 10-350g/l.
7, according to each the method for claim 1-6, add when being characterised in that the silicate of step (c) and souring agent and undertaken: join silicate in the medium continuously by following manner, pH regulates by introducing souring agent in the interpolation process, if the pH of medium is higher than the set controlling valu of 7-8.
8, according to each the method for claim 1-6, add when being characterised in that the silicate of step (c) and souring agent and undertaken: join silicate in the medium continuously by following manner, pH regulates by introducing silicate in the interpolation process, if the pH of medium is lower than the trial value of 7-8.
9, according to each the method for claim 1-6, add when being characterised in that the silicate of step (c) and souring agent and comprise continuous interpolation souring agent and silicate, wherein calculating concentration and flow velocity make to remain on 7-8 at the pH of whole interpolation process medium.
10,, be characterised in that the silicate introduced in the interpolation process exists with the form of the aqueous solution of concentration with 10-360g/l in step (c) according to each the method for claim 1-9.
11,, be characterised in that the souring agent introduced in the interpolation process exists with the form of the centinormal 1 aqueous solution with 0.25-8N in step (c) according to each the method for claim 1-10.
12,, be characterised in that the interpolation of step (c) continues 15-300 minute according to each the method for claim 1-11.
13,, be characterised in that at the end of step (c) and/or between step (c) and step (e), aluminum compound be incorporated in the medium according to each the method for claim 1-12.
14,, be characterised in that and use step (d), and be the souring agent of step (d) form with the centinormal 1 aqueous solution with 0.25-8N is incorporated in the medium according to each the method for claim 1-13.
15,, be characterised in that step (a) and (b), (c) and (d) under 90-100 ℃ temperature, carry out according to each the method for claim 1-14.
16, according to each the method for claim 1-15, be characterised in that before, will carry out maturation stage by the aqueous silica dispersion that step (d) obtains in step (e).
17, according to each the method for claim 1-16, be characterised in that step (e) comprises the technology that divides precipitated filter cakes.
18, pass through the water-based silicon dioxide compositions of the splitting method acquisition of claim 17.
19, each the method by claim 1-17 obtains, or is lower than the precipitated silica of 6% water-intake rate according to having of obtaining of the silicon dioxide compositions of claim 18 by spraying drying.
20, each the method by claim 1-17 obtains, or the precipitated silica that obtains according to the silicon dioxide compositions of claim 18 by spraying drying is as the purposes of the reinforcing filler in the silicone type matrix.
21, according to the purposes of claim 20, wherein silicone type matrix is by extruding moulding.
22, each the method by claim 1-17 obtains, or the precipitated silica that obtains according to the silicon dioxide compositions of claim 18 by spraying drying is as the purposes based on the reinforcing filler in the matrix of one or more elastomericss.
23,, be characterised in that the described matrix based on one or more elastomericss is transparent or semitransparent matrix according to the purposes of claim 21.
24, each the method by claim 1-17 obtains, or the precipitated silica that obtains according to the silicon dioxide compositions of claim 18 by spraying drying is as the purposes of the thickening material in organic or aqueous medium.
25, each the method by claim 1-17 obtains, or the precipitated silica that obtains according to the silicon dioxide compositions of claim 18 by spraying drying is as the purposes of the carrier in food or the make-up composition.
26, each the method by claim 1-17 obtains, or the precipitated silica that obtains according to the silicon dioxide compositions of claim 18 by spraying drying is as the purposes of the filler in the pharmaceutical composition, carrier and/or excipient.
27, comprise that each method by claim 1-17 obtains, or the pharmaceutical composition of the precipitated silica that obtains according to the silicon dioxide compositions of claim 18 by spraying drying.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR01/16881 | 2001-12-26 | ||
| FR0116881A FR2833937B1 (en) | 2001-12-26 | 2001-12-26 | SILICA WITH LOW WATER RESUME |
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| Publication Number | Publication Date |
|---|---|
| CN1617833A true CN1617833A (en) | 2005-05-18 |
| CN100497171C CN100497171C (en) | 2009-06-10 |
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|---|---|---|---|
| CNB028276280A Expired - Fee Related CN100497171C (en) | 2001-12-26 | 2002-12-24 | Low water absorption silicon-dioxide |
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|---|---|
| US (1) | US7524478B2 (en) |
| EP (1) | EP1458646B1 (en) |
| JP (1) | JP4538224B2 (en) |
| KR (1) | KR100805257B1 (en) |
| CN (1) | CN100497171C (en) |
| AT (1) | ATE533731T1 (en) |
| AU (1) | AU2002364341A1 (en) |
| BR (1) | BR0215357B1 (en) |
| CA (1) | CA2471416C (en) |
| ES (1) | ES2377559T3 (en) |
| FR (1) | FR2833937B1 (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101402457B (en) * | 2007-11-05 | 2011-04-13 | 通化双龙化工股份有限公司 | Process for producing deposition white carbon black for silicon rubber |
| CN111573683A (en) * | 2020-07-09 | 2020-08-25 | 福建省南平嘉茂纳米科技发展有限公司 | Preparation method of silica with high specific surface area and low oil absorption value and product thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2818966B1 (en) * | 2000-12-28 | 2003-03-07 | Rhodia Chimie Sa | PROCESS FOR THE PREPARATION OF PRECIPITATED SILICA CONTAINING ALUMINUM |
| FR2862978B1 (en) | 2003-12-01 | 2005-12-30 | Rhodia Chimie Sa | NOVEL ADHERENCE PROMOTING AGENT ON A THERMAL INSULATING SURFACE AND IN PARTICULAR ON A POLYSTYRENE SURFACE, AND ITS USE IN THE FIELD OF CONSTRUCTION AND ESPECIALLY IN ISOLATION SYSTEMS |
| FR2864098B1 (en) * | 2003-12-19 | 2007-08-31 | Rhodia Chimie Sa | FLAME RETARDANT SYSTEM COMPRISING PHOSPHORUS COMPOUNDS AND FLAME RETARDANT POLYMER COMPOSITION |
| FR2864063B1 (en) * | 2003-12-19 | 2006-04-07 | Rhodia Chimie Sa | HIGH STRUCTURE SILICA WITH LOW WATER RESISTANCE |
| NO20040167L (en) * | 2004-01-14 | 2005-07-15 | Cod Technologies As | Process for producing precipitated silica from olivine |
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2001
- 2001-12-26 FR FR0116881A patent/FR2833937B1/en not_active Expired - Fee Related
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2002
- 2002-12-24 MX MXPA04006240A patent/MXPA04006240A/en active IP Right Grant
- 2002-12-24 KR KR1020047010195A patent/KR100805257B1/en active IP Right Grant
- 2002-12-24 CA CA2471416A patent/CA2471416C/en not_active Expired - Fee Related
- 2002-12-24 JP JP2003556344A patent/JP4538224B2/en not_active Expired - Fee Related
- 2002-12-24 BR BRPI0215357-2A patent/BR0215357B1/en not_active IP Right Cessation
- 2002-12-24 ES ES02799118T patent/ES2377559T3/en not_active Expired - Lifetime
- 2002-12-24 EP EP02799118A patent/EP1458646B1/en not_active Expired - Lifetime
- 2002-12-24 AT AT02799118T patent/ATE533731T1/en active
- 2002-12-24 WO PCT/FR2002/004559 patent/WO2003055801A1/en active Application Filing
- 2002-12-24 CN CNB028276280A patent/CN100497171C/en not_active Expired - Fee Related
- 2002-12-24 US US10/500,107 patent/US7524478B2/en not_active Expired - Fee Related
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101402457B (en) * | 2007-11-05 | 2011-04-13 | 通化双龙化工股份有限公司 | Process for producing deposition white carbon black for silicon rubber |
| CN111573683A (en) * | 2020-07-09 | 2020-08-25 | 福建省南平嘉茂纳米科技发展有限公司 | Preparation method of silica with high specific surface area and low oil absorption value and product thereof |
| CN111573683B (en) * | 2020-07-09 | 2021-12-28 | 福建省南平嘉茂纳米科技发展有限公司 | Preparation method of silica with high specific surface area and low oil absorption value and product thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1458646A1 (en) | 2004-09-22 |
| WO2003055801A1 (en) | 2003-07-10 |
| BR0215357A (en) | 2004-12-14 |
| CN100497171C (en) | 2009-06-10 |
| BR0215357B1 (en) | 2012-02-22 |
| AU2002364341A1 (en) | 2003-07-15 |
| EP1458646B1 (en) | 2011-11-16 |
| CA2471416A1 (en) | 2003-07-10 |
| FR2833937A1 (en) | 2003-06-27 |
| MXPA04006240A (en) | 2004-11-01 |
| US7524478B2 (en) | 2009-04-28 |
| JP4538224B2 (en) | 2010-09-08 |
| KR100805257B1 (en) | 2008-02-20 |
| ATE533731T1 (en) | 2011-12-15 |
| ES2377559T3 (en) | 2012-03-28 |
| CA2471416C (en) | 2010-09-21 |
| FR2833937B1 (en) | 2004-11-12 |
| US20050074386A1 (en) | 2005-04-07 |
| JP2005512935A (en) | 2005-05-12 |
| KR20040076875A (en) | 2004-09-03 |
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